The DABCO-catalysed Baylis-Hillman reactions in the chloroaluminate room temperature ionic liquids: Rate promoting and recyclable media

Journal of Molecular Catalysis A: Chemical

Volumn 211, Issue 1-2, 2004, Pages 43-47

  Kumar, Anil ^a   Pawar, Sanjay S ^a  

^a NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

Baylis Hillman reaction; DABCO; Ionic liquid; Rates

Indexed keywords

AROMATIC COMPOUNDS; THERMAL EFFECTS;

IONIC LIQUIDS;

CATALYSIS;

1,4 DIAZABICYCLO[2.2.2]OCTANE; ALUMINUM DERIVATIVE; CHLOROALUMINATE; ION; UNCLASSIFIED DRUG;

ARTICLE; BAYLIS HILLMAN REACTION; CATALYSIS; LIQUID; REACTION ANALYSIS; RECYCLING; ROOM TEMPERATURE;

EID: 0942300627     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2003.10.002     Document Type: Article

References (44)

1. A.B. Baylis, M.E.D. Hillman, German Patent 2155113 (1972); Chem. Abstr. 77 (1972) 34174q.
2. Drewes S.E., Roos G.H.P. Tetrahedron. 44:1988;4653.
3. Basavaiah D., Rao P.D., Hyma R.S. Tetrahedron. 52:1996;8001.
4. Ciganek E. Org. React. 51:1997;201.
5. Langer P. Angew. Chem. Int. Ed. 39:2000;3049.
6. Ameer F., Drewes S.E., Freese S., Kaye P.T. Synth. Commun. 18:1988;495.
7. J.S. Hill, N.S. Isaacs, J. Chem. Res. (S) (1988) 330.
8. Roos G.H.P., Ramprasadh P. Synth. Commun. 21:1993;1261.
9. Auge J., Lubin N., Lubineau A. Tetrahedron Lett. 35:1994;7947.
10. M.K. Kundu, S.B. Mukherjee, N. Balu, R. Padmakumar, S. Bhat, Synlett. (1994) 444.
11. Oshi T., Oguri H., Hirama M. Tetrahedron: Asymmetry. 6:1995;1241.
12. Rafel S., Leahy J.W. J. Org. Chem. 62:1997;1521.
13. V.K. Aggarwal, A. Mereu, Chem. Commun. (1999) 2311.
14. Kawamura M., Kobayashi S. Tetrahedron Lett. 40:1999;1539.
15. Yu C., Liu B., Hu L. J. Org. Chem. 66:2001;5413.
16. Aggarwal V.K., Dean D.K., Mereu A., Williams R. J. Org. Chem. 67:2002;510.
17. Basavaih D., Rao A.J., Satyanarayana T. Chem. Rev. 103:2003;811.
18. Kumar A., Pawar S.S. Tetrahedron. 59:2003;5019.
19. Seddon K.R. Kinet. Catal. 37:1996;693.
20. Seddon K.R. J. Chem. Technol. Biotechnol. 68:1997;351.
21. M. Freemantle, C&E News (1998) (March 30) 32.
22. Welton T. Chem. Rev. 99:1999;2071.
23. Wassercheid P., Wilhelm K. Angew. Chem. Int. Ed. 39:2000;3772.
24. R. Sheldon. Chem. Commun. (2001) 2399.
25. Gordon M. Appl. Catal. A: Gen. 222:2001;101.
26. Hussey C.L. Pure & Appl. Chem. 60:1988;1763. and references cited therein.
27. Lee C.W. Tetrahedron Lett. 40:1999;2461.
28. A. Kumar, S.S. Pawar, J. Mol. Catal. A (2003), in press, available as advance article on WEB.
29. Boob J.A., Levisky J.A., Pflug J.L., Wilkes J.S. J. Org. Chem. 51:1986;480.
30. Goledzinowski M., Biriss V.I. Ind. Eng. Chem. Res. 32:1993;1795.
31. Tang J., Osteryoung R. Synth. Met. 45:1991;1.
32. J.K.D. Surette, L. Green, R.D. Singer, J. Chem. Soc., Chem. Commun. (1996) 2753.
33. P.J. Dyson, M.C. Grossel, N. Srinivasan, T. Vine, T. Welton, D.J. Williams, A.J.P. White, T. Zigras, J. Chem. Soc., Dalton Trans. (1997) 3465.
34. Rosa J.N., Afonso C.A.M., Santos A.G. Tetrahedron. 57:2001;4189.
35. V.K. Aggarwal, I. Emme, A. Mereu, Chem. Commun. (2002) 1621.
36. Kim E.J., Ko S.Y., Song C.E. Helv. Chim. Acta. 86:2003;894.
37. Kabalka G.W., Venkataiah B., Dong G. Tetrahedron Lett. 44:2003;4473.
38. G.L. Rebeiro, B.M. Khadilkar, Synthesis (2001) 370.
39. Perry R.L., Jones K.M., Scott W.D., Liao Q., Hussey C.L. J. Chem. Eng. Data. 40:1995;615.
40. Robinson J., Osteryoung R.A. J. Am. Chem. Soc. 101:1979;323.
41. Chang N.-H., Grimmett R.M. Aust. J. Chem. 30:1977;2005.
42. Shi M., Jiang J.-K., Feng Y.-S. Organic Lett. 2:2000;2397.
43. Shi M., Jiang J.-K., Cui S.-C., Feng Y.-S. J. Chem. Soc., Perkin Trans. 1:2001;394.
44. M. Shi, C.-Q. Li, J.-K. Jiang, Chem. Commun. (2001) 835.